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二十二碳六烯酸(DHA)饮食干预对载脂蛋白E缺陷型和C57BL/6J野生型小鼠肝脏脂质代谢的影响。

Effects of DHA dietary intervention on hepatic lipid metabolism in apolipoprotein E-deficient and C57BL/6J wild-type mice.

作者信息

Xu Jingjing, Guo Yujie, Huang Xiaochen, Ma Xiaojun, Li Pengfei, Wang Ying, Wang Xixiang, Yuan Linhong

机构信息

School of Public Health, Capital Medical University, Beijing 100069, PR China.

The Affiliated Suzhou Science and Technology Town Hospital of Nanjing Medical University, Suzhou, Jiangsu 215153, PR China.

出版信息

Biomed Pharmacother. 2021 Dec;144:112329. doi: 10.1016/j.biopha.2021.112329. Epub 2021 Oct 13.

Abstract

Lipid metabolic disorder occurs when ApoE gene is deficient. However, the role of Docosahexaenoic acid (DHA) in relieving hepatic lipid metabolic disorder in apolipoprotein E-deficient (ApoE -/-) mice remains unknown. We fed 3-month-old C57BL/6J wild-type (C57 wt) and ApoE -/- mice respectively with normal or DHA fortified diet for 5 months. We found ApoE gene deficiency caused hepatic lipid deposition and increased lipid levels in plasma and liver. Hepatic gene expression of SRB1, CD36 and FABP5 in ApoE -/- mice, protein expression of HMGCR, LRP1 in C57 wt mice and protein expression of LRP1 in ApoE -/- mice increased after DHA intervention. In DHA-fed ApoE -/- mice, LXRα/β and PPARα protein expression down-regulated in cytoplasm, but LXRα/β protein expression up-regulated in nucleus. DHA treatment decreased RXRα and RXRβ expression in C57 wt and ApoE -/- female mice. Deletion of ApoE gene caused lipid metabolism disorder in liver of mice. DHA treatment efficiently meliorated lipid metabolism caused by ApoE deficient through the regulation of gene and protein expressions of molecules involved in liver fatty acids transport and lipid metabolism.

摘要

载脂蛋白E(ApoE)基因缺陷时会发生脂质代谢紊乱。然而,二十二碳六烯酸(DHA)在缓解载脂蛋白E缺陷(ApoE -/-)小鼠肝脏脂质代谢紊乱中的作用尚不清楚。我们分别给3个月大的C57BL/6J野生型(C57 wt)和ApoE -/-小鼠喂食正常或富含DHA的饮食5个月。我们发现ApoE基因缺陷导致肝脏脂质沉积,并使血浆和肝脏中的脂质水平升高。DHA干预后,ApoE -/-小鼠肝脏中SRB1、CD36和FABP5的基因表达,C57 wt小鼠中HMGCR、LRP1的蛋白表达以及ApoE -/-小鼠中LRP1的蛋白表达均增加。在喂食DHA的ApoE -/-小鼠中,LXRα/β和PPARα蛋白在细胞质中的表达下调,但LXRα/β蛋白在细胞核中的表达上调。DHA处理降低了C57 wt和ApoE -/-雌性小鼠中RXRα和RXRβ的表达。ApoE基因缺失导致小鼠肝脏脂质代谢紊乱。DHA处理通过调节肝脏脂肪酸转运和脂质代谢相关分子的基因和蛋白表达,有效改善了由ApoE缺陷引起的脂质代谢。

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